SPACELINE HIGH VOLUME EVACUATION HANDPIE— 510(k) K801682

Name: FDA 510(k) clearance K801682
Creator: U.S. Food and Drug Administration
Published: 1980-08-04

Substantially Equivalent

Pacific Dental Corp.

FDA 510(k) clearance K801682 for SPACELINE HIGH VOLUME EVACUATION HANDPIE, Substantially Equivalent on 1980-08-04. Applicant: Pacific Dental Corp.. Device class: 1.

Clearance details

Applicant: Pacific Dental Corp.
Product code: Code EHZ
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 1980-07-21
Decision date: 1980-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.